13 results for author:"Storch A." in Literature citations
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| Chorein-sensitive polymerization of cortical actin and suicidal cell death in chorea-acanthocytosis. Foller M., Hermann A., Gu S., Alesutan I., Qadri S.M., Borst O., Schmidt E.M., Schiele F., vom Hagen J.M., Saft C. et al. FASEB J. 26:1526-1534(2012) · Mapped (2) |
| An SK3 channel/nWASP/Abi-1 complex is involved in early neurogenesis. Liebau S., Steinestel J., Linta L., Kleger A., Storch A., Schoen M., Steinestel K., Proepper C., Bockmann J., Schmeisser M.J. et al. PLoS ONE 6:e18148-e18148(2011) · Mapped (2) |
| Modulation of calcium-activated potassium channels induces cardiogenesis of pluripotent stem cells and enrichment of pacemaker-like cells. Kleger A., Seufferlein T., Malan D., Tischendorf M., Storch A., Wolheim A., Latz S., Protze S., Porzner M., Proepper C. et al. Circulation 122:1823-1836(2010) · Mapped (3) |
| Genome-wide expression profiling and functional network analysis upon neuroectodermal conversion of human mesenchymal stem cells suggest HIF-1 and miR-124a as important regulators. Maisel M., Habisch H.J., Royer L., Herr A., Milosevic J., Hermann A., Liebau S., Brenner R., Schwarz J., Schroeder M. et al. Exp. Cell Res. 316:2760-2778(2010) · Mapped (1) |
| Altered migration and adhesion potential of pro-neurally converted human bone marrow stromal cells. Habisch H.J., Fiedler J., Ludolph A.C., Storch A., Brenner R.E. Cytotherapy 10:824-833(2008) · Mapped (4) |
| GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak. Weber Y.G., Storch A., Wuttke T.V., Brockmann K., Kempfle J., Maljevic S., Margari L., Kamm C., Schneider S.A., Huber S.M. et al. J. Clin. Invest. 118:2157-2168(2008) · UniProtKB (1) · Mapped (5) |
| A novel mutation (c.64_65delGGinsAACC [p.G21fsX66]) in the GTP cyclohydrolase 1 gene that causes Segawa disease. von Mering M., Gabriel H., Opladen T., Hoffmann G.F., Storch A. J. Neurol. Neurosurg. Psychiatr. 79:229-229(2008) · Mapped (5) |
| Formation of cellular projections in neural progenitor cells depends on SK3 channel activity. Liebau S., Vaida B., Proepper C., Grissmer S., Storch A., Boeckers T.M., Dietl P., Wittekindt O.H. J. Neurochem. 101:1338-1350(2007) · Mapped (6) |
| Lack of hypoxia-inducible factor-1 alpha impairs midbrain neural precursor cells involving vascular endothelial growth factor signaling. Milosevic J., Maisel M., Wegner F., Leuchtenberger J., Wenger R.H., Gerlach M., Storch A., Schwarz J. J. Neurosci. 27:412-421(2007) · Mapped (12) |
| Dopamine transporter-mediated cytotoxicity of 6-hydroxydopamine in vitro depends on expression of mutant alpha-synucleins related to Parkinson's disease. Lehmensiek V., Tan E.M., Liebau S., Lenk T., Zettlmeisl H., Schwarz J., Storch A. Neurochem. Int. 48:329-340(2006) · Mapped (10) |
| Mutational spectrum of the CHAC gene in patients with chorea-acanthocytosis. Dobson-Stone C., Danek A., Rampoldi L., Hardie R.J., Chalmers R.M., Wood N.W., Bohlega S., Dotti M.T., Federico A., Shizuka M. et al. Eur. J. Hum. Genet. 10:773-781(2002) · UniProtKB (1) |
| Expression of mutant alpha-synucleins enhances dopamine transporter-mediated MPP+ toxicity in vitro. Lehmensiek V., Tan E.M., Schwarz J., Storch A. Neuroreport 13:1279-1283(2002) · Mapped (7) |
| FTDP-17: an early-onset phenotype with parkinsonism and epileptic seizures caused by a novel mutation. Sperfeld A.D., Collatz M.B., Baier H., Palmbach M., Storch A., Schwarz J., Tatsch K., Reske S., Joosse M., Heutink P. et al. Ann. Neurol. 46:708-715(1999) · UniProtKB (1) |